159 related articles for article (PubMed ID: 17110374)
1. Insertion and topology of normal and mutant bestrophin-1 in the endoplasmic reticulum membrane.
Milenkovic VM; Rivera A; Horling F; Weber BH
J Biol Chem; 2007 Jan; 282(2):1313-21. PubMed ID: 17110374
[TBL] [Abstract][Full Text] [Related]
2. [VMD2 and its role in Best's disease and other retinopathies].
Stöhr H; Milenkowic V; Weber BH
Ophthalmologe; 2005 Feb; 102(2):116-21. PubMed ID: 15627199
[TBL] [Abstract][Full Text] [Related]
3. [Function of bestrophin].
Strauss O; Rosenthal R
Ophthalmologe; 2005 Feb; 102(2):122-6. PubMed ID: 15627200
[TBL] [Abstract][Full Text] [Related]
4. Molecular evolution and functional divergence of the bestrophin protein family.
Milenkovic VM; Langmann T; Schreiber R; Kunzelmann K; Weber BH
BMC Evol Biol; 2008 Feb; 8():72. PubMed ID: 18307799
[TBL] [Abstract][Full Text] [Related]
5. New VMD2 gene mutations identified in patients affected by Best vitelliform macular dystrophy.
Marchant D; Yu K; Bigot K; Roche O; Germain A; Bonneau D; Drouin-Garraud V; Schorderet DF; Munier F; Schmidt D; Le Neindre P; Marsac C; Menasche M; Dufier JL; Fischmeister R; Hartzell C; Abitbol M
J Med Genet; 2007 Mar; 44(3):e70. PubMed ID: 17287362
[TBL] [Abstract][Full Text] [Related]
6. The mutation spectrum of the bestrophin protein--functional implications.
Bakall B; Marknell T; Ingvast S; Koisti MJ; Sandgren O; Li W; Bergen AA; Andreasson S; Rosenberg T; Petrukhin K; Wadelius C
Hum Genet; 1999 May; 104(5):383-9. PubMed ID: 10394929
[TBL] [Abstract][Full Text] [Related]
7. The vitelliform macular dystrophy protein defines a new family of chloride channels.
Sun H; Tsunenari T; Yau KW; Nathans J
Proc Natl Acad Sci U S A; 2002 Mar; 99(6):4008-13. PubMed ID: 11904445
[TBL] [Abstract][Full Text] [Related]
8. The gene causing the Best's macular dystrophy (BMD) encodes a putative ion exchanger.
Gómez A; Cedano J; Oliva B; Piñol J; Querol E
DNA Seq; 2001 Dec; 12(5-6):431-5. PubMed ID: 11913792
[TBL] [Abstract][Full Text] [Related]
9. The anion-selective pore of the bestrophins, a family of chloride channels associated with retinal degeneration.
Qu Z; Chien LT; Cui Y; Hartzell HC
J Neurosci; 2006 May; 26(20):5411-9. PubMed ID: 16707793
[TBL] [Abstract][Full Text] [Related]
10. Disease-associated missense mutations in bestrophin-1 affect cellular trafficking and anion conductance.
Milenkovic VM; Röhrl E; Weber BH; Strauss O
J Cell Sci; 2011 Sep; 124(Pt 17):2988-96. PubMed ID: 21878505
[TBL] [Abstract][Full Text] [Related]
11. Molecular physiology of bestrophins: multifunctional membrane proteins linked to best disease and other retinopathies.
Hartzell HC; Qu Z; Yu K; Xiao Q; Chien LT
Physiol Rev; 2008 Apr; 88(2):639-72. PubMed ID: 18391176
[TBL] [Abstract][Full Text] [Related]
12. Human disease-causing mutations disrupt an N-C-terminal interaction and channel function of bestrophin 1.
Qu Z; Cheng W; Cui Y; Cui Y; Zheng J
J Biol Chem; 2009 Jun; 284(24):16473-16481. PubMed ID: 19372599
[TBL] [Abstract][Full Text] [Related]
13. A potential cytosolic function of bestrophin-1.
Strauss O; Neussert R; Müller C; Milenkovic VM
Adv Exp Med Biol; 2012; 723():603-10. PubMed ID: 22183384
[No Abstract] [Full Text] [Related]
14. Clinical expression of Best's vitelliform macular dystrophy in Swedish families with mutations in the bestrophin gene.
Ponjavic V; Eksandh L; Andréasson S; Sjöström K; Bakall B; Ingvast S; Wadelius C; Ehinger B
Ophthalmic Genet; 1999 Dec; 20(4):251-7. PubMed ID: 10617923
[TBL] [Abstract][Full Text] [Related]
15. A novel mutation in the VMD2 gene in an Italian family with Best maculopathy.
Sodi A; Passerini I; Simonelli F; Testa F; Menchini U; Torricelli F
J Fr Ophtalmol; 2007 Jun; 30(6):616-20. PubMed ID: 17646752
[TBL] [Abstract][Full Text] [Related]
16. Bestrophin gene mutations in patients with Best vitelliform macular dystrophy.
Caldwell GM; Kakuk LE; Griesinger IB; Simpson SA; Nowak NJ; Small KW; Maumenee IH; Rosenfeld PJ; Sieving PA; Shows TB; Ayyagari R
Genomics; 1999 May; 58(1):98-101. PubMed ID: 10331951
[TBL] [Abstract][Full Text] [Related]
17. Dbest1, a Drosophila homolog of human Bestrophin, is not required for viability or photoreceptor integrity.
Tavsanli BC; Pappu KS; Mehta SQ; Mardon G
Genesis; 2001 Nov; 31(3):130-6. PubMed ID: 11747204
[TBL] [Abstract][Full Text] [Related]
18. Evaluation of the Best disease gene in patients with age-related macular degeneration and other maculopathies.
Allikmets R; Seddon JM; Bernstein PS; Hutchinson A; Atkinson A; Sharma S; Gerrard B; Li W; Metzker ML; Wadelius C; Caskey CT; Dean M; Petrukhin K
Hum Genet; 1999 Jun; 104(6):449-53. PubMed ID: 10453731
[TBL] [Abstract][Full Text] [Related]
19. Bestrophin, the product of the Best vitelliform macular dystrophy gene (VMD2), localizes to the basolateral plasma membrane of the retinal pigment epithelium.
Marmorstein AD; Marmorstein LY; Rayborn M; Wang X; Hollyfield JG; Petrukhin K
Proc Natl Acad Sci U S A; 2000 Nov; 97(23):12758-63. PubMed ID: 11050159
[TBL] [Abstract][Full Text] [Related]
20. Modeling the structural consequences of BEST1 missense mutations.
Guziewicz KE; Aguirre GD; Zangerl B
Adv Exp Med Biol; 2012; 723():611-8. PubMed ID: 22183385
[No Abstract] [Full Text] [Related]
[Next] [New Search]
